氧化趋化肽N-甲酰-L-蛋氨酰-亚砜-L-亮氨酰-L-苯丙氨酸的酶促还原 - Suppr

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超能文献

Enzymatic reduction of oxidized chemotactic peptide N-formyl-L-methionyl-sulfoxide-L-leucyl-L-phenylalanine.

作者信息

Fliss H, Vasanthakumar G, Schiffmann E, Weissbach H, Brot N

出版信息

Biochem Biophys Res Commun. 1982 Nov 16;109(1):194-201. doi: 10.1016/0006-291x(82)91584-4.

DOI:10.1016/0006-291x(82)91584-4

PMID:6760863

Abstract

摘要

相似文献

Enzymatic reduction of oxidized chemotactic peptide N-formyl-L-methionyl-sulfoxide-L-leucyl-L-phenylalanine.氧化趋化肽N-甲酰-L-蛋氨酰-亚砜-L-亮氨酰-L-苯丙氨酸的酶促还原

Biochem Biophys Res Commun. 1982 Nov 16;109(1):194-201. doi: 10.1016/0006-291x(82)91584-4.

Human granulocytes and granulocytes from other species demonstrate differences in chemotactic responsiveness to oxidized N-formyl-methionyl-leucyl-phenylalanine.人类粒细胞和其他物种的粒细胞对氧化型N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸的趋化反应性存在差异。

Comp Biochem Physiol A Comp Physiol. 1989;92(1):97-100. doi: 10.1016/0300-9629(89)90748-2.

Purification and identification of formyl-methionyl-leucyl-phenylalanine as the major peptide neutrophil chemotactic factor produced by Escherichia coli.将甲酰甲硫氨酰亮氨酰苯丙氨酸纯化并鉴定为大肠杆菌产生的主要肽中性粒细胞趋化因子。

J Biol Chem. 1984 May 10;259(9):5430-9.

Oxidation of n-formyl methionyl chemotactic peptide by human neutrophils.人中性粒细胞对N-甲酰甲硫氨酰趋化肽的氧化作用。

J Immunol. 1981 Apr;126(4):1387-9.

Antibacterial and immunostimulatory properties of chemotactic N-formyl peptide conjugates of ampicillin and amoxicillin.氨苄西林和阿莫西林趋化性N-甲酰肽缀合物的抗菌和免疫刺激特性

Antimicrob Agents Chemother. 1989 Sep;33(9):1516-21. doi: 10.1128/AAC.33.9.1516.

Human neutrophil Fc gamma RIIIB and formyl peptide receptors are functionally linked during formyl-methionyl-leucyl-phenylalanine-induced chemotaxis.在甲酰甲硫氨酰亮氨酰苯丙氨酸诱导的趋化作用过程中，人中性粒细胞FcγRIIIB和甲酰肽受体在功能上相互关联。

J Immunol. 1992 Aug 1;149(3):989-97.

Retro-all-D and retro isomers of a formyl-methionyl peptide chemoattractant: an insight into the mode of binding at the receptor on rabbit neutrophils.一种甲酰甲硫氨酰肽趋化因子的全反式-D型和反式异构体：对兔中性粒细胞受体结合模式的深入了解。

Biochim Biophys Acta. 1986 Dec 10;884(3):545-9. doi: 10.1016/0304-4165(86)90206-0.

Chemotactic peptide binding by intact neutrophils from human neonates.人类新生儿完整中性粒细胞对趋化肽的结合

Pediatr Res. 1984 Jan;18(1):63-6.

Suppressive effect of rebamipide, an antiulcer agent, against activation of human neutrophils exposed to formyl-methionyl-leucyl-phenylalanine.抗溃疡药物瑞巴派特对暴露于甲酰甲硫氨酰亮氨酰苯丙氨酸的人中性粒细胞激活的抑制作用。

Histol Histopathol. 2000 Oct;15(4):1067-76. doi: 10.14670/HH-15.1067.

The synthetic chemotactic peptide formyl-methionyl-leucyl-phenylalanine causes an increase in actin associated with the cytoskeleton in rabbit neutrophils.合成趋化肽甲酰甲硫氨酰亮氨酰苯丙氨酸会使兔中性粒细胞中与细胞骨架相关的肌动蛋白增加。

Biochem Biophys Res Commun. 1982 Oct 15;108(3):1144-9. doi: 10.1016/0006-291x(82)92120-9.

引用本文的文献

Bacterial peptide methionine sulphoxide reductase: co-induction with glutathione S-transferase during chemical stress conditions.细菌肽甲硫氨酸亚砜还原酶：在化学应激条件下与谷胱甘肽S-转移酶共同诱导。

Biochem J. 2001 Dec 15;360(Pt 3):675-81. doi: 10.1042/0264-6021:3600675.

Cloning the expression of a mammalian gene involved in the reduction of methionine sulfoxide residues in proteins.克隆一个参与蛋白质中甲硫氨酸亚砜残基还原的哺乳动物基因的表达。

Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2095-9. doi: 10.1073/pnas.93.5.2095.

Chromosomal localization of the mammalian peptide-methionine sulfoxide reductase gene and its differential expression in various tissues.哺乳动物肽-蛋氨酸亚砜还原酶基因的染色体定位及其在不同组织中的差异表达。

Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3205-8. doi: 10.1073/pnas.93.8.3205.

Physical map location of the peptide methionine sulfoxide reductase gene on the Escherichia coli chromosome.肽甲硫氨酸亚砜还原酶基因在大肠杆菌染色体上的物理图谱定位。

J Bacteriol. 1994 Mar;176(5):1548-9. doi: 10.1128/jb.176.5.1548-1549.1994.

Escherichia coli peptide methionine sulfoxide reductase gene: regulation of expression and role in protecting against oxidative damage.大肠杆菌肽甲硫氨酸亚砜还原酶基因：表达调控及在抵御氧化损伤中的作用

J Bacteriol. 1995 Feb;177(3):502-7. doi: 10.1128/jb.177.3.502-507.1995.

Oxidation of methionine residues in proteins of activated human neutrophils.活化的人中性粒细胞蛋白质中蛋氨酸残基的氧化

Proc Natl Acad Sci U S A. 1983 Dec;80(23):7160-4. doi: 10.1073/pnas.80.23.7160.

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